US20060289303A1 - Ito sputtering target - Google Patents

Ito sputtering target Download PDF

Info

Publication number
US20060289303A1
US20060289303A1 US10/569,068 US56906806A US2006289303A1 US 20060289303 A1 US20060289303 A1 US 20060289303A1 US 56906806 A US56906806 A US 56906806A US 2006289303 A1 US2006289303 A1 US 2006289303A1
Authority
US
United States
Prior art keywords
ito
particles
sputtering target
target
etching
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US10/569,068
Other versions
US7504351B2 (en
Inventor
Toshiya Kurihara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JX Nippon Mining and Metals Corp
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Assigned to NIKKO MATERIALS CO., LTD. reassignment NIKKO MATERIALS CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KURIHARA, TOSHIYA
Assigned to NIPPON MINING & METALS CO., LTD. reassignment NIPPON MINING & METALS CO., LTD. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: NIKKO MATERIALS CO., LTD.
Publication of US20060289303A1 publication Critical patent/US20060289303A1/en
Application granted granted Critical
Publication of US7504351B2 publication Critical patent/US7504351B2/en
Assigned to JX NIPPON MINING & METALS CORPORATION reassignment JX NIPPON MINING & METALS CORPORATION CHANGE OF NAME/MERGER Assignors: NIPPON MINING & METALS CO., LTD.
Assigned to JX NIPPON MINING & METALS CORPORATION reassignment JX NIPPON MINING & METALS CORPORATION CHANGE OF ADDRESS Assignors: JX NIPPON MINING & METALS CORPORATION
Assigned to JX NIPPON MINING & METALS CORPORATION reassignment JX NIPPON MINING & METALS CORPORATION CHANGE OF ADDRESS Assignors: JX NIPPON MINING & METALS CORPORATION
Active legal-status Critical Current
Adjusted expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/3407Cathode assembly for sputtering apparatus, e.g. Target
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/34Sputtering
    • C23C14/3407Cathode assembly for sputtering apparatus, e.g. Target
    • C23C14/3414Metallurgical or chemical aspects of target preparation, e.g. casting, powder metallurgy
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/54Controlling or regulating the coating process
    • C23C14/548Controlling the composition

Definitions

  • the present invention relates to an ITO (compound oxide having indium and tin as primary components: In 2 O 3 —SnO 2 ) sputtering target to be used in forming an ITO film.
  • ITO compound oxide having indium and tin as primary components: In 2 O 3 —SnO 2
  • An ITO film is widely used as a transparent electrode (film) of a display device; mainly a liquid crystal display.
  • this ITO film As a method of forming this ITO film, ordinarily employed is a method generally referred to as a physical vapor deposition method such as the vacuum deposition method or sputtering method. Particularly, the magnetron sputtering method is often employed for forming such ITO film from the perspective of operability and stability of the film.
  • a physical vapor deposition method such as the vacuum deposition method or sputtering method.
  • the magnetron sputtering method is often employed for forming such ITO film from the perspective of operability and stability of the film.
  • the formation of film with the sputtering method is performed by physically colliding a positive ion such as Ar ion to a target established in the negative electrode, discharging materials composing the target with such collision energy, and laminating films of approximately the same composition as the target material on the substrate on the opposing positive electrode side.
  • the coating method employing the sputtering method is characterized in that it is capable of forming from a thin film of angstrom units to a thick film of several ten ⁇ m at a stable deposition speed by adjusting the processing time, power supply, and so on.
  • a particular problem in forming an ITO film is the generation of minute protrusions referred to as nodules on the target surface during the sputtering operation, which increases pursuant to the increase in sputtering time.
  • Nodules generate arcing during sputtering, and fragments of nodules or reducing substances of ITO become particles and are dispersed. When such dispersions adhere to the ITO film, that portion will become defective, and cause the productivity to deteriorate.
  • the target surface was purified or smoothed, or the high densification of the target was sought.
  • the most effective method was to uniformly disperse tin oxide in the raw material powder (e.g., refer to Patent Document 1).
  • Patent Document 1 International Publication No. WO2002072912
  • an object of the present invention is to provide an ITO (compound oxide having indium and tin as primary components: In 2 O 3 —SnO 2 ) sputtering target capable of inhibiting the generation of arcing in the sputtering process of forming a transparent electrode film or the like, suppressing the generation of defects of the ITO film caused by such arcing, and reducing the formation of nodules and abnormal discharge.
  • ITO compound oxide having indium and tin as primary components: In 2 O 3 —SnO 2
  • the present invention provides:
  • An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 1 particle/ ⁇ m 2 or less;
  • An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.2 particles/ ⁇ m 2 or less;
  • the ITO sputtering target according to claim 1 wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.02 particles/ ⁇ m 2 or less;
  • ITO sputtering target according to claim 4 wherein particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching or sputter etching do not exist in the target.
  • the ITO target of the present invention As a result of using the ITO target of the present invention, a significant effect is yielded in that the generation of arcing can be inhibited in the sputter deposition process, defects in the ITO film caused by such arcing can be suppressed, and deterioration in the ITO film can be inhibited as a result thereof.
  • FIG. 1 is an SEM image (magnification of 5000) of the sputtered surface of an ITO target in which the sintering temperature is high (1550 to 1600° C.);
  • FIG. 2 is an SEM image (magnification of 50000) of the inner-granular microstructures of an ITO target in which the sintering temperature is high (1550 to 1600° C.) and the sputter etching speed is slow;
  • FIG. 3 is a diagram showing the sintering temperature dependency of the minimum retention time ( ⁇ ) in which the sintering density becomes 7.12 g/cm 3 or greater, maximum retention time ( ⁇ ) in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/ ⁇ m 2 or less, and maximum retention temperature ( ⁇ ) in which the number of particles becomes 0.02 particles/ ⁇ m 2 or less;
  • FIG. 4 is an SEM image (magnification of 20000) of inner-granular microstructures of an ITO target in which the sintering temperature is high (1550 to 1600° C.);
  • FIG. 5 is an SEM image (magnification of 20000) of inner-granular microstructures of an ITO target in which the sintering temperature is low (1470 to 1500° C.);
  • FIG. 6 is an SEM image (magnification of 20000, magnification of 50000) of the sintered body used in Example 2;
  • FIG. 7 is an SEM image (magnification of 20000, magnification of 50000) of the sintered body used in Comparative Example 1;
  • FIG. 8 is a diagram showing the accumulated number of arcings during the sputtering of the ITO target used in the Examples and Comparative Examples.
  • etching via sputtering is not conducted uniformly on the target surface, and that microstructures having a size of roughly 500 nm or less and having a comparatively slow etching speed exist inside grains.
  • FIG. 1 and FIG. 2 show an SEM image of the ITO target surface etched via sputtering.
  • minute grains can be observed in the crystalline structure shown with magnification of 5000 structure.
  • FIG. 2 is an enlargement thereof at magnification of 50000.
  • the minute particles of 100 nm or less observed in FIG. 2 is considered to be an area with high tin content. These minute particles have a slower etching speed in comparison to other structures. Thus, these minute particles are left behind during sputtering, and it is easy to image that these are either discharged from the target as foreign matter, or generate minute arcing and thereby cause defects in the ITO film.
  • microstructures are not caused by the non-uniformity (segregation) of tin oxide in the raw material powder, but are rather substances arising in the normal manufacturing method of an ITO sintered body.
  • the condition of these microstructures depends on the maximum temperature during sintering, and it has become clear that the higher the sintering temperature, the larger the particles, and the number of particles would increase as a result thereof.
  • the sintering temperature is the same, it has become clear that lower the tin oxide composition, the smaller the particles. Therefore, in order to reduce or minify the minute particles having a slow etching speed, it is necessary to lower the sintering temperature, or to reduce the tin oxide composition. Nevertheless, if the sintering temperature is lowered, sintering cannot be performed sufficiently, and it will be difficult to increase the density of the ITO target.
  • An ITO target having a low density generates nodules and arcing during sputtering, and fragments of nodules or reducing substances of ITO become particles and are dispersed. When such dispersions adhere to the ITO film, that portion will become defective, and cause the productivity to deteriorate.
  • an ITO sintered body is obtained by mixing indium oxide powder and tin oxide powder as the raw materials to become a prescribed composition, molding this, and sintering the obtained compact in an oxygen atmosphere.
  • the indium oxide powder and tin oxide powder as the raw materials must have an appropriate specific surface area.
  • oxide raw material powder or the mixed powder thereof must be dry- or wet-pulverized to increase the specific surface area. Thereby, the sinterability of the raw material powder is improved even more, and it becomes easier to increase the sintering density even with a low sintering temperature.
  • the holding time during the maximum temperature in sintering it is necessary to take particular note on the holding time during the maximum temperature in sintering. If the holding time during the maximum temperature is too short, a high sintering density cannot be obtained, and, if this is too long, it will assist in the growth of particles, and an appropriate holding time must be adopted. In other words, the lower limit of holding time during the maximum sintering temperature is limited based on the sintering density, and the upper limit thereof is limited based on the size of particles.
  • FIG. 3 shows the scope of sintering conditions of a sintered body prepared using the raw material powder with improved sinterability with the method described above in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/ ⁇ m 2 or less and the sintering density becomes 7.12 g/cm 3 or greater, and the sintering conditions in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.02 particles/ ⁇ m 2 or less and the sintering density becomes 7.12 g/cm 3 or greater.
  • the sintering temperature being less than 1450° C., it was not possible to obtain a sintered body having a density of 7.12 g/cm 3 or greater. With the sintering temperature exceeding 1550° C., it was not possible to obtain a sintered body in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/ ⁇ m 2 or less.
  • the sintering temperature is low, although it will be easy to obtain a sintered body having few particles that are 100 nm or greater, the sintering time will be long in order to obtain a sintering density of 7.12 g/cm 3 or greater, and the productivity will deteriorate. Further, if the sintering temperature is high, although it will be easy to obtain a high density sintered body, the sintering conditions for obtaining a sintered body with few particles that are 100 nm or greater will become narrow, and the level of defectiveness will increase. The sintering conditions during actual production should be decided in consideration of the above.
  • the lower limit there is 8.5 wt. % or higher, and more desirably 9.0 wt. % or higher.
  • FIG. 4 is an SEM image of the surface of the ITO target sintered at a maximum temperature of 1550 to 1600° C., and thereafter subject to royal water etching. Numerous minute particles of 100 nm or greater exist after the etching. In order to reduce such minute particles, it is necessary to change the sintering conditions or the tin oxide composition.
  • the present invention in light of the foregoing circumstances, enables the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 1 particle/ ⁇ m 2 or less. As a result, it is possible to considerably reduce the generation of arcing in comparison to conventional targets.
  • the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 0.2 particles/ ⁇ m 2 or less.
  • the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 0.02 particles/ ⁇ m 2 or less.
  • particles having a grain diameter of 1 ⁇ m or greater exposed as a result of royal water etching or sputter etching do not exist in the target, preferably particles having a grain diameter of 100 nm or greater do not exist in the target, and more preferably particles having an average grain size of 10 nm or greater do not exist in the target.
  • particles having a grain diameter of 1 ⁇ m or greater exposed as a result of royal water etching or sputter etching do not exist in the target, preferably particles having a grain diameter of 100 nm or greater do not exist in the target, and more preferably particles having an average grain size of 10 nm or greater do not exist in the target.
  • the sintering temperature is low, although it will be easy to obtain a sintered body having few particles that are 100 nm or greater, the sintering time will be long in order to obtain a sintering density of 7.12 g/cm 3 or greater, and the productivity will deteriorate. Further, if the sintering temperature is high, although it will be easy to obtain a high density sintered body, the sintering conditions for obtaining a sintered body with few particles that are 100 nm or greater will become narrow, and the level of defectiveness will increase. The sintering conditions during actual production should be decided in consideration of the above.
  • FIG. 5 is an SEM image of the surface of the ITO target sintered at a maximum temperature of 1470 to 1550° C., and thereafter subject to sputter etching.
  • An ITO sintered at a low temperature clearly has a smooth surface with no inner-granular microstructures of low etching speed, or which are extremely minute at 100 nm or less.
  • microstructures of roughly 100 nm can be confirmed at a maximum sintering temperature of 1550° C. or higher, and can hardly be observed at a maximum sintering temperature of 1550° C. or less, and it can no longer be observed at a temperature of 1470° C. or less.
  • the target density was respectively 7.129, 7.130 and 7.132 g/cm 3 .
  • the number of particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching was respectively 0.02, 0.19, and 0.80 particles/ ⁇ m 2 .
  • FIG. 6 shows an SEM image of the etched face of the 0.19 particles/ ⁇ m 2 .
  • these sintered targets were used to form a transparent electrode film under the following conditions by performing DC magnetron sputtering to a glass substrate.
  • the integral power consumption of sputtering was discharged up to 160 Whr/cm 2 .
  • the generation (coverage) of nodules in this was measured, and the coverage of nodules on the target face was respectively 0.12%, 0.11% and 0.09%.
  • the number of accumulated arcings in which the discharge energy is 10 mJ or less was respectively 31, 35 and 48.
  • the solid line in FIG. 8 shows the change in the number of accumulated arcings pursuant to the integral power consumption of the Examples.
  • the compacts obtained with the same method as Examples 1 to 3 were sintered in an oxygen atmosphere at a maximum temperature of 1530° C. to 1620° C. so as to be outside the sintering conditions shown in FIG. 3 , and the obtained sintered bodies were subject to machining in order to obtain ITO targets.
  • the target density was respectively 7.132 g/cm 3 and 7.133 g/cm 3 .
  • the number of particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching was respectively 1.1 particles/ ⁇ m 2 and 1.3 particles/ ⁇ m 2 .
  • FIG. 7 shows an SEM image of the etched face of the 1.1 particles/ ⁇ m 2 .
  • This target was used to conduct a discharge test with DC magnetron sputtering under the same conditions as Example 1 until the integral power consumption of sputtering became 160 Whr/cm 2 , and the coverage of nodules on the target surface was respectively 0.11% and 0.12%.
  • the number of accumulated arcings in which the discharge energy is 10 mJ or less was 150 and 213.
  • the dotted line in FIG. 8 shows the change in the number of accumulated arcings pursuant to the integral power consumption of the Comparative Examples.
  • Table 1 shows a list of the target density, number of particles that are 100 ⁇ m or greater, nodule coverage during sputtering, and number of arcings of Examples 1 to 3 and Comparative Examples 1 and 2 of the present invention.
  • the ITO target of the present invention yields a superior effect in that it is able to inhibit the generation of arcing, suppress the generation of defects in the ITO film caused by such arcing, and inhibit the deterioration of the ITO film.
  • TABLE 1 Number of Particles Number of 100 nm or Nodule Arcings Density Larger Coverage (number Sample (g/cm 3 ) (particles/ ⁇ m 2 ) (%) of times)
  • Example 1 7.129 0.015 0.12 31
  • Example 2 7.130 0.19 0.11 35
  • Example 3 7.132 0.80 0.09 48

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physical Vapour Deposition (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

Provided are an ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 1 particle/μm2, and an ITO sputtering target having a density of 7.12 g/cm3 or greater capable of improving the sputtering performance, in particular inhibiting the generation of arcing, suppressing the generation of defects in the ITO film caused by such arcing, and thereby effectively inhibiting the deterioration of the ITO film.

Description

    TECHNICAL FIELD
  • The present invention relates to an ITO (compound oxide having indium and tin as primary components: In2O3—SnO2) sputtering target to be used in forming an ITO film.
  • BACKGROUND ART
  • An ITO film is widely used as a transparent electrode (film) of a display device; mainly a liquid crystal display.
  • As a method of forming this ITO film, ordinarily employed is a method generally referred to as a physical vapor deposition method such as the vacuum deposition method or sputtering method. Particularly, the magnetron sputtering method is often employed for forming such ITO film from the perspective of operability and stability of the film.
  • The formation of film with the sputtering method is performed by physically colliding a positive ion such as Ar ion to a target established in the negative electrode, discharging materials composing the target with such collision energy, and laminating films of approximately the same composition as the target material on the substrate on the opposing positive electrode side.
  • The coating method employing the sputtering method is characterized in that it is capable of forming from a thin film of angstrom units to a thick film of several ten μm at a stable deposition speed by adjusting the processing time, power supply, and so on.
  • A particular problem in forming an ITO film is the generation of minute protrusions referred to as nodules on the target surface during the sputtering operation, which increases pursuant to the increase in sputtering time.
  • Nodules generate arcing during sputtering, and fragments of nodules or reducing substances of ITO become particles and are dispersed. When such dispersions adhere to the ITO film, that portion will become defective, and cause the productivity to deteriorate.
  • Due to the foregoing reasons, upon the actual manufacture, it is necessary to periodically remove the nodules generated on the target surface. This, however, causes problems in the considerable deterioration of productivity, and a target generating few nodules is being demanded.
  • Conventionally, in order to reduce nodules, the target surface was purified or smoothed, or the high densification of the target was sought. The most effective method was to uniformly disperse tin oxide in the raw material powder (e.g., refer to Patent Document 1).
  • As a result of this method, it is possible to reduce as much as possible the segregation in the tin oxide target having low conductivity and low sputter etching speed, and thereby reduce defects in the ITO film caused by arcing resulting from the generation of nodules.
  • Nevertheless, in recent years, for the advancement of high resolution of flat panel displays and improvement in the production yield of ITO films, even small defects can no longer be ignored, and demands for further reducing the arcing are increasing.
  • [Patent Document 1] International Publication No. WO2002072912
  • DISCLOSURE OF THE INVENTION
  • Thus, an object of the present invention is to provide an ITO (compound oxide having indium and tin as primary components: In2O3—SnO2) sputtering target capable of inhibiting the generation of arcing in the sputtering process of forming a transparent electrode film or the like, suppressing the generation of defects of the ITO film caused by such arcing, and reducing the formation of nodules and abnormal discharge.
  • The present invention provides:
  • 1. An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 1 particle/μm2 or less;
  • 2. An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.2 particles/μm2 or less;
  • 3. The ITO sputtering target according to claim 1, wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.02 particles/μm2 or less;
  • 4. The ITO sputtering target according to any one of claims 1 to 3, wherein particles having a grain diameter of 1 μm or greater exposed as a result of royal water etching or sputter etching do not exist in the target;
  • 5. The ITO sputtering target according to claim 4, wherein particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching or sputter etching do not exist in the target.
  • 6. The ITO sputtering target according to claim 5, wherein particles having a grain diameter of 10 nm or greater exposed as a result of royal water etching or sputter etching do not exist in the target; and
  • 7. The ITO sputtering target according to any one of claims 1 to 6, wherein the density is 7.12 g/cm3 or greater.
  • [Effect of the Invention]
  • As a result of using the ITO target of the present invention, a significant effect is yielded in that the generation of arcing can be inhibited in the sputter deposition process, defects in the ITO film caused by such arcing can be suppressed, and deterioration in the ITO film can be inhibited as a result thereof.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is an SEM image (magnification of 5000) of the sputtered surface of an ITO target in which the sintering temperature is high (1550 to 1600° C.);
  • FIG. 2 is an SEM image (magnification of 50000) of the inner-granular microstructures of an ITO target in which the sintering temperature is high (1550 to 1600° C.) and the sputter etching speed is slow;
  • FIG. 3 is a diagram showing the sintering temperature dependency of the minimum retention time (∘) in which the sintering density becomes 7.12 g/cm3 or greater, maximum retention time (□) in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/μm2 or less, and maximum retention temperature (Δ) in which the number of particles becomes 0.02 particles/μm2 or less;
  • FIG. 4 is an SEM image (magnification of 20000) of inner-granular microstructures of an ITO target in which the sintering temperature is high (1550 to 1600° C.);
  • FIG. 5 is an SEM image (magnification of 20000) of inner-granular microstructures of an ITO target in which the sintering temperature is low (1470 to 1500° C.);
  • FIG. 6 is an SEM image (magnification of 20000, magnification of 50000) of the sintered body used in Example 2;
  • FIG. 7 is an SEM image (magnification of 20000, magnification of 50000) of the sintered body used in Comparative Example 1; and
  • FIG. 8 is a diagram showing the accumulated number of arcings during the sputtering of the ITO target used in the Examples and Comparative Examples.
  • BEST MODE FOR CARRYING OUT THE INVENTION
  • In order to realize the further reduction of arcing, as a result of conducting a detailed observation of the sputtered face of the ITO target, the present inventors discovered that etching via sputtering is not conducted uniformly on the target surface, and that microstructures having a size of roughly 500 nm or less and having a comparatively slow etching speed exist inside grains.
  • FIG. 1 and FIG. 2 show an SEM image of the ITO target surface etched via sputtering. In FIG. 1, minute grains can be observed in the crystalline structure shown with magnification of 5000 structure. FIG. 2 is an enlargement thereof at magnification of 50000.
  • In particular, the minute particles of 100 nm or less observed in FIG. 2 is considered to be an area with high tin content. These minute particles have a slower etching speed in comparison to other structures. Thus, these minute particles are left behind during sputtering, and it is easy to image that these are either discharged from the target as foreign matter, or generate minute arcing and thereby cause defects in the ITO film.
  • As a result of conducting further study on these inner-granular microstructures, it has become evident that such microstructures are not caused by the non-uniformity (segregation) of tin oxide in the raw material powder, but are rather substances arising in the normal manufacturing method of an ITO sintered body.
  • Further, with an ITO in which the tin oxide composition is 10 wt. % and which most generally used for flat panel displays, the condition of these microstructures depends on the maximum temperature during sintering, and it has become clear that the higher the sintering temperature, the larger the particles, and the number of particles would increase as a result thereof.
  • Further, even if the sintering temperature is the same, it has become clear that lower the tin oxide composition, the smaller the particles. Therefore, in order to reduce or minify the minute particles having a slow etching speed, it is necessary to lower the sintering temperature, or to reduce the tin oxide composition. Nevertheless, if the sintering temperature is lowered, sintering cannot be performed sufficiently, and it will be difficult to increase the density of the ITO target.
  • An ITO target having a low density generates nodules and arcing during sputtering, and fragments of nodules or reducing substances of ITO become particles and are dispersed. When such dispersions adhere to the ITO film, that portion will become defective, and cause the productivity to deteriorate.
  • Therefore, not only lowering the sintering temperature, but also not lowering the sintering density is necessary.
  • Generally, an ITO sintered body is obtained by mixing indium oxide powder and tin oxide powder as the raw materials to become a prescribed composition, molding this, and sintering the obtained compact in an oxygen atmosphere.
  • In order to decrease the sintering temperature without lowering the sintering density, it is necessary to sufficiently examine the processes, and improve the sinterability. Thus, the indium oxide powder and tin oxide powder as the raw materials must have an appropriate specific surface area.
  • Further, oxide raw material powder or the mixed powder thereof must be dry- or wet-pulverized to increase the specific surface area. Thereby, the sinterability of the raw material powder is improved even more, and it becomes easier to increase the sintering density even with a low sintering temperature.
  • Moreover, upon obtaining a compact from raw material powder, it is necessary to obtain a high density compact by using cold isostatic pressing (CIP) and to adopt a compact retention method where the oxygen atmosphere will get across the entire compact during sintering.
  • Further, it is necessary to take particular note on the holding time during the maximum temperature in sintering. If the holding time during the maximum temperature is too short, a high sintering density cannot be obtained, and, if this is too long, it will assist in the growth of particles, and an appropriate holding time must be adopted. In other words, the lower limit of holding time during the maximum sintering temperature is limited based on the sintering density, and the upper limit thereof is limited based on the size of particles.
  • FIG. 3 shows the scope of sintering conditions of a sintered body prepared using the raw material powder with improved sinterability with the method described above in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/μm2 or less and the sintering density becomes 7.12 g/cm3 or greater, and the sintering conditions in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.02 particles/μm2 or less and the sintering density becomes 7.12 g/cm3 or greater.
  • With the sintering temperature being less than 1450° C., it was not possible to obtain a sintered body having a density of 7.12 g/cm3 or greater. With the sintering temperature exceeding 1550° C., it was not possible to obtain a sintered body in which the number of particles of 100 nm or greater exposed as a result of royal water etching is 0.2 particles/μm2 or less.
  • As shown in FIG. 3, if the sintering temperature is low, although it will be easy to obtain a sintered body having few particles that are 100 nm or greater, the sintering time will be long in order to obtain a sintering density of 7.12 g/cm3 or greater, and the productivity will deteriorate. Further, if the sintering temperature is high, although it will be easy to obtain a high density sintered body, the sintering conditions for obtaining a sintered body with few particles that are 100 nm or greater will become narrow, and the level of defectiveness will increase. The sintering conditions during actual production should be decided in consideration of the above.
  • Further, even if the sintering temperature is the same, the lower the tin oxide composition, the smaller the particles, but it becomes difficult to increase the sintering density. Moreover, characteristics of the ITO film prepared from such a target will change significantly.
  • Therefore, simply reducing the tin oxide composition will not be sufficient, and it is desirable that the lower limit there is 8.5 wt. % or higher, and more desirably 9.0 wt. % or higher.
  • Incidentally, even in etching (25° C. for 3 minutes) using royal water (volume ratio is HCl: HNO3:H2O=1:0.08:1), microstructures having a slow etching speed as with the etching surface via sputtering will become exposed. Therefore, the etching surface using royal water is the same as the etching surface via sputter etching. Since similar results can be obtained by preparing a small tablet shaped sample and subjecting this to royal water etching, the time required for evaluating the etching face can be shortened than by producing a target and subjecting this to sputter etching.
  • FIG. 4 is an SEM image of the surface of the ITO target sintered at a maximum temperature of 1550 to 1600° C., and thereafter subject to royal water etching. Numerous minute particles of 100 nm or greater exist after the etching. In order to reduce such minute particles, it is necessary to change the sintering conditions or the tin oxide composition.
  • The present invention, in light of the foregoing circumstances, enables the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 1 particle/μm2 or less. As a result, it is possible to considerably reduce the generation of arcing in comparison to conventional targets.
  • Further, it is desirable to make the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 0.2 particles/μm2 or less.
  • Moreover, further still, it is desirable to make the number of particles having a grain diameter of 100 nm or greater existing in the ITO sputtering target exposed as a result of royal water etching or sputtering etching to be 0.02 particles/μm2 or less.
  • In addition, it is preferable that particles having a grain diameter of 1 μm or greater exposed as a result of royal water etching or sputter etching do not exist in the target, preferably particles having a grain diameter of 100 nm or greater do not exist in the target, and more preferably particles having an average grain size of 10 nm or greater do not exist in the target. As a result, it is possible to reduce the generation of arcing as much as possible.
  • As shown in FIG. 3, if the sintering temperature is low, although it will be easy to obtain a sintered body having few particles that are 100 nm or greater, the sintering time will be long in order to obtain a sintering density of 7.12 g/cm3 or greater, and the productivity will deteriorate. Further, if the sintering temperature is high, although it will be easy to obtain a high density sintered body, the sintering conditions for obtaining a sintered body with few particles that are 100 nm or greater will become narrow, and the level of defectiveness will increase. The sintering conditions during actual production should be decided in consideration of the above.
  • FIG. 5 is an SEM image of the surface of the ITO target sintered at a maximum temperature of 1470 to 1550° C., and thereafter subject to sputter etching.
  • An ITO sintered at a low temperature clearly has a smooth surface with no inner-granular microstructures of low etching speed, or which are extremely minute at 100 nm or less.
  • As shown with the sintering conditions of FIG. 3, microstructures of roughly 100 nm can be confirmed at a maximum sintering temperature of 1550° C. or higher, and can hardly be observed at a maximum sintering temperature of 1550° C. or less, and it can no longer be observed at a temperature of 1470° C. or less.
  • As described above, by performing sputtering with an ITO target having no inner-granular microstructures of a low etching speed or which are extremely minute having an average grain size of 100 nm or less, it is possible to effectively inhibit the generation of arcing in comparison to conventional targets, suppress the generation of particles caused by such arcing, and effectively inhibit the deterioration of the ITO film.
  • EXAMPLES
  • Examples of the present invention are now explained. These Examples are merely illustrative, and the present invention shall in no way be limited thereby. In other words, the present invention shall only be limited by the scope of the present invention, and shall include the various modifications other than the Examples of this invention.
  • Examples 1 to 3
  • After mixing indium oxide powder 90 wt. % and tin oxide powder 10 wt %, this was pulverized with a bead mill in wet process until the increase of the specific surface area became 2.5 m2/g, and then a binder was added and dried. This dry powder was press molded at a pressure of 500 kgf cm2, and this was further subject to cold isostatic pressing (CIP) of 2 ton/cm2 in order to obtain a compact of 650×180×9 mm.
  • Those compacts were sintered in an oxygen atmosphere at a maximum temperature of 1470° C. to 1500° C. so as to satisfy the sintering conditions shown in FIG. 3, and the obtained sintered bodies were subject to machining in order to obtain ITO targets.
  • The target density was respectively 7.129, 7.130 and 7.132 g/cm3. The number of particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching was respectively 0.02, 0.19, and 0.80 particles/μm2. FIG. 6 shows an SEM image of the etched face of the 0.19 particles/μm2.
  • Next, these sintered targets were used to form a transparent electrode film under the following conditions by performing DC magnetron sputtering to a glass substrate.
  • Sputter gas: Ar+O2 (99:1)
  • Sputter gas pressure: 0.5 Pa
  • Electric energy: 60 W
  • Sputter output: 0.5 W/cm2
  • As a result of the above, the integral power consumption of sputtering was discharged up to 160 Whr/cm2. The generation (coverage) of nodules in this was measured, and the coverage of nodules on the target face was respectively 0.12%, 0.11% and 0.09%. Further, the number of accumulated arcings in which the discharge energy is 10 mJ or less was respectively 31, 35 and 48. The solid line in FIG. 8 shows the change in the number of accumulated arcings pursuant to the integral power consumption of the Examples.
  • Comparative Example 1, 2
  • The compacts obtained with the same method as Examples 1 to 3 were sintered in an oxygen atmosphere at a maximum temperature of 1530° C. to 1620° C. so as to be outside the sintering conditions shown in FIG. 3, and the obtained sintered bodies were subject to machining in order to obtain ITO targets.
  • The target density was respectively 7.132 g/cm3 and 7.133 g/cm3. The number of particles having a grain diameter of 100 nm or greater exposed as a result of royal water etching was respectively 1.1 particles/μm2 and 1.3 particles/μm2. FIG. 7 shows an SEM image of the etched face of the 1.1 particles/μm2.
  • This target was used to conduct a discharge test with DC magnetron sputtering under the same conditions as Example 1 until the integral power consumption of sputtering became 160 Whr/cm2, and the coverage of nodules on the target surface was respectively 0.11% and 0.12%.
  • Further, the number of accumulated arcings in which the discharge energy is 10 mJ or less was 150 and 213. The dotted line in FIG. 8 shows the change in the number of accumulated arcings pursuant to the integral power consumption of the Comparative Examples.
  • As shown in FIG. 8, the number of accumulated arcings of Examples 1 to 3 is clearly superior to that of the Comparative Examples.
  • Table 1 shows a list of the target density, number of particles that are 100 μm or greater, nodule coverage during sputtering, and number of arcings of Examples 1 to 3 and Comparative Examples 1 and 2 of the present invention.
  • The ITO target of the present invention yields a superior effect in that it is able to inhibit the generation of arcing, suppress the generation of defects in the ITO film caused by such arcing, and inhibit the deterioration of the ITO film.
    TABLE 1
    Number of
    Particles Number of
    100 nm or Nodule Arcings
    Density Larger Coverage (number
    Sample (g/cm3) (particles/μm2) (%) of times)
    Example 1 7.129 0.015 0.12 31
    Example 2 7.130 0.19 0.11 35
    Example 3 7.132 0.80 0.09 48
    Comparative 7.132 1.10 0.11 150
    Example 1
    Comparative 7.133 1.30 0.12 213
    Example 2

Claims (11)

1. An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 1 particle/μm2 or less and wherein particles having a grain diameter of 1 μm or greater do not exist in the target.
2. An ITO sputtering target wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.2 particle/μm2 or less and wherein particles having a grain diameter of 1 μm or greater do not exist in the target.
3. The ITO sputtering target according to claim 1, wherein the number of particles having a grain diameter of 100 nm or greater exposed in the ITO sputtering target as a result of royal water etching or sputter etching is 0.02 particle/μm2 or less.
4-7. (canceled)
8. An ITO sputtering target according to claim 3, wherein the ITO sputtering target has a density of 7.12 g/cm3 or greater.
9. An ITO sputtering target according to claim 2, wherein the ITO sputtering target has a density of 7.12 g/cm3 or greater.
10. An ITO sputtering target according to claim 1, wherein the ITO sputtering target has a density of 7.12 g/cm3 or greater.
11. An ITO sputtering target wherein said ITO sputtering target has no particle having a grain diameter of 100 nm or greater exposed on the ITO sputtering target as a result of royal water etching or sputter etching.
12. An ITO sputtering target according to claim 11, wherein the ITO sputtering target has a density of 7.12 g/cm3 or greater.
13. An ITO sputtering target according to claim 11, wherein said ITO sputtering target has no particle having a grain diameter of 10 nm or greater exposed on the ITO sputtering target as a result of royal water etching or sputter etching.
14. An ITO sputtering target according to claim 13, wherein the ITO sputtering target has a density of 7.12 g/cm3 or greater.
US10/569,068 2003-08-20 2004-08-04 ITO sputtering target Active 2025-02-09 US7504351B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2003=296077 2003-08-20
JP2003296077 2003-08-20
PCT/JP2004/011153 WO2005019492A1 (en) 2003-08-20 2004-08-04 Ito sputtering target

Publications (2)

Publication Number Publication Date
US20060289303A1 true US20060289303A1 (en) 2006-12-28
US7504351B2 US7504351B2 (en) 2009-03-17

Family

ID=34213582

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/569,068 Active 2025-02-09 US7504351B2 (en) 2003-08-20 2004-08-04 ITO sputtering target

Country Status (6)

Country Link
US (1) US7504351B2 (en)
JP (1) JP4813182B2 (en)
KR (1) KR100727242B1 (en)
CN (1) CN100489150C (en)
TW (1) TWI290178B (en)
WO (1) WO2005019492A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11081326B2 (en) * 2016-07-11 2021-08-03 Semiconductor Energy Laboratory Co., Ltd. Sputtering target and method for manufacturing the same

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003050324A1 (en) * 2001-12-03 2003-06-19 Nippon Sheet Glass Company, Limited Method for forming thin film, substrate having thin film formed by the method, and photoelectric conversion device using the substrate
JP4562664B2 (en) * 2006-02-07 2010-10-13 三井金属鉱業株式会社 ITO sintered body and ITO sputtering target
JP2007211265A (en) * 2006-02-07 2007-08-23 Mitsui Mining & Smelting Co Ltd Ito sintered body and ito sputtering target
JP5091414B2 (en) * 2006-03-14 2012-12-05 三井金属鉱業株式会社 ITO sintered body, sputtering target material, sputtering target, and method for producing sputtering target material
KR20100012040A (en) * 2007-06-26 2010-02-04 닛코 킨조쿠 가부시키가이샤 Amorphous composite oxide film,crystalline composite oxide film,process for producing amorphous composite oxide film,process for producing crystalline composite oxide film,and composite oxide sinter
WO2009011232A1 (en) 2007-07-13 2009-01-22 Nippon Mining & Metals Co., Ltd. Composite oxide sinter, process for producing amorphous composite oxide film, amorphous composite oxide film, process for producing crystalline composite oxide film, and crystalline composite oxide film
JP5202630B2 (en) * 2008-06-10 2013-06-05 Jx日鉱日石金属株式会社 Oxide sintered compact target for sputtering and manufacturing method thereof
US9214253B2 (en) 2009-10-26 2015-12-15 Jx Nippon Mining & Metals Corporation Sintered compact of indium oxide system, and transparent conductive film of indium oxide system

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5980815A (en) * 1996-12-20 1999-11-09 Tosoh Corporation Process for producing ITO sintered body
US6106681A (en) * 1997-10-13 2000-08-22 Japan Energy Corporation ITO sputtering target and its cleaning method
US6121178A (en) * 1996-10-04 2000-09-19 Dowa Mining Co., Ltd. Sintered ITO and an ITO sputtering target
US6929772B2 (en) * 2001-03-28 2005-08-16 Nikko Materials Co., Ltd. Manufacturing method of ito powder with tin dissolved in indium oxide, and manufacturing method of ito target

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05247636A (en) 1992-03-06 1993-09-24 Hitachi Metals Ltd Sputtering target for indium-tin oxide film and manufacture therefor
JP3457969B2 (en) 1992-05-11 2003-10-20 東ソー株式会社 High density ITO sintered body and sputtering target
JP3324164B2 (en) * 1992-12-25 2002-09-17 東ソー株式会社 Indium oxide powder, method for producing the same, and method for producing ITO sintered body
JP3676961B2 (en) 1999-04-02 2005-07-27 株式会社日鉱マテリアルズ Tin oxide-indium oxide powder for forming ITO film and sputtering target for forming ITO film
JP4190888B2 (en) 2001-03-12 2008-12-03 日鉱金属株式会社 Tin oxide powder for ITO sputtering target, method for producing the same, and method for producing sintered sputtering target for forming ITO film
JP2003171761A (en) 2001-12-10 2003-06-20 Nikko Materials Co Ltd Ito sputtering target having reduced occurrence quantity of nodule

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6121178A (en) * 1996-10-04 2000-09-19 Dowa Mining Co., Ltd. Sintered ITO and an ITO sputtering target
US5980815A (en) * 1996-12-20 1999-11-09 Tosoh Corporation Process for producing ITO sintered body
US6106681A (en) * 1997-10-13 2000-08-22 Japan Energy Corporation ITO sputtering target and its cleaning method
US6929772B2 (en) * 2001-03-28 2005-08-16 Nikko Materials Co., Ltd. Manufacturing method of ito powder with tin dissolved in indium oxide, and manufacturing method of ito target

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11081326B2 (en) * 2016-07-11 2021-08-03 Semiconductor Energy Laboratory Co., Ltd. Sputtering target and method for manufacturing the same
TWI754542B (en) * 2016-07-11 2022-02-01 日商半導體能源研究所股份有限公司 Sputtering target and metal oxide
US11735403B2 (en) 2016-07-11 2023-08-22 Semiconductor Energy Laboratory Co., Ltd. Sputtering target and method for manufacturing the same

Also Published As

Publication number Publication date
JPWO2005019492A1 (en) 2007-11-22
TW200510554A (en) 2005-03-16
CN1839215A (en) 2006-09-27
KR100727242B1 (en) 2007-06-11
JP4813182B2 (en) 2011-11-09
TWI290178B (en) 2007-11-21
KR20060038472A (en) 2006-05-03
WO2005019492A1 (en) 2005-03-03
CN100489150C (en) 2009-05-20
US7504351B2 (en) 2009-03-17

Similar Documents

Publication Publication Date Title
EP2278041B1 (en) Sputtering target and transparent conductive film obtainable by the target
US9202603B2 (en) Sputtering target, transparent conductive film and transparent electrode
US8920683B2 (en) Sputtering target, transparent conductive film and transparent electrode
US7569167B2 (en) Oxide sintered body
JP4850378B2 (en) Sputtering target, transparent conductive oxide, and method for producing sputtering target
JP5686067B2 (en) Zn-Sn-O-based oxide sintered body and method for producing the same
JP4947942B2 (en) Sputtering target
JPH10306367A (en) Zno-ga2o3 sintered body for sputtering target and its production
JP2006347807A (en) Oxide sintered compact, oxide transparent conductive film, and method for manufacturing the same
US20040222089A1 (en) Sputtering target and transparent electroconductive film
JP2007250369A (en) Transparent conductive film and its manufacturing method
US7504351B2 (en) ITO sputtering target
JP4234483B2 (en) ITO sputtering target, manufacturing method thereof, and ITO transparent conductive film
JP3782355B2 (en) ITO sputtering target
JP4794757B2 (en) Sputtering target for forming a transparent electrode film
JPH10297963A (en) Zno-ga2o3-based sintered compact for sputtering target and production of the sintered compact
JP2001072470A (en) Production of ito sintered compact
JP2001262326A (en) Indium oxide-metallic thin powder mixture, ito sputtering target using the same powdery mixture as raw material and method for producing the same target
JP2001335925A (en) Method for producing ito thin film
JP5822034B2 (en) Sputtering target and manufacturing method thereof

Legal Events

Date Code Title Description
AS Assignment

Owner name: NIKKO MATERIALS CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:KURIHARA, TOSHIYA;REEL/FRAME:018344/0124

Effective date: 20060213

AS Assignment

Owner name: NIPPON MINING & METALS CO., LTD.,JAPAN

Free format text: CHANGE OF NAME;ASSIGNOR:NIKKO MATERIALS CO., LTD.;REEL/FRAME:018560/0126

Effective date: 20060403

Owner name: NIPPON MINING & METALS CO., LTD., JAPAN

Free format text: CHANGE OF NAME;ASSIGNOR:NIKKO MATERIALS CO., LTD.;REEL/FRAME:018560/0126

Effective date: 20060403

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: JX NIPPON MINING & METALS CORPORATION, JAPAN

Free format text: CHANGE OF NAME/MERGER;ASSIGNOR:NIPPON MINING & METALS CO., LTD.;REEL/FRAME:026417/0023

Effective date: 20101221

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

AS Assignment

Owner name: JX NIPPON MINING & METALS CORPORATION, JAPAN

Free format text: CHANGE OF ADDRESS;ASSIGNOR:JX NIPPON MINING & METALS CORPORATION;REEL/FRAME:041649/0733

Effective date: 20160104

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1553); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 12

AS Assignment

Owner name: JX NIPPON MINING & METALS CORPORATION, JAPAN

Free format text: CHANGE OF ADDRESS;ASSIGNOR:JX NIPPON MINING & METALS CORPORATION;REEL/FRAME:057160/0114

Effective date: 20200629